Project Management - Clinical Research

The professional in this role will plan, coordinate, and oversee clinical trial support projects, ensuring that timelines, budgets, and quality standards are met. Day-to-day responsibilities include managing project plans, tracking progress and risks, coordinating with internal teams and external stakeholders, and maintaining clear documentation and reporting. The role involves aligning supply chain activities with trial requirements, supporting regulatory and logistical planning, and proactively resolving operational issues. Collaboration with cross-functional teams and clients will be key to ensuring reliable delivery of devices, equipment, and ancillary supplies to trial sites.
Qualifications
Candidates should possess strong Project Management and Program Management skills for coordinating complex clinical research and supply chain initiatives.
Candidates should possess solid Project Planning and organizational skills to develop timelines, manage resources, and ensure on-time delivery of project milestones.
Candidates should possess excellent Analytical Skills to interpret data, assess risks, and support decision-making in clinical operations and logistics.
Candidates should possess clear and professional Communication skills for collaborating with cross-functional teams, vendors, and clients across global regions.
Relevant experience in clinical research, clinical operations, or clinical supply chain management is highly beneficial.
Familiarity with regulatory and quality standards in drug development and medical devices is an advantage.

Work arrangement
Yes